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AFFIRM (TM) VCF SYSTEM

K110998 Class II Traditional
Decision Date
2011-10-25
Sponsor / Applicant
Algea Therapies

Technical Specification

510(k) Submission ID K110998
Product Code NDN
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3027
Decision Date 2011-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AFFIRM (TM) VCF SYSTEM received FDA 510(k) clearance under submission number K110998, sponsored by Algea Therapies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-10-25.

Classification & Regulation

This clearance is catalogued under FDA product code NDN and 21 CFR 888.3027, within the Orthopedic review panel as a Class II device.